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Membrane Surface-EnhancedRaman Spectroscopy for Cholesterol-Modified Lipid Systems: Effectof Gold Nanoparticle Size

机译:膜表面增强胆固醇修饰脂质系统的拉曼光谱:效果金纳米颗粒尺寸

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摘要

A gold nanoparticle (AuNP) has a localized surface plasmon resonance peak depending on its size, which is often utilized for surface-enhanced Raman scattering (SERS). To obtain information on the cholesterol (Chol)-incorporated lipid membranes by SERS, AuNPs (5, 100 nm) were first functionalized by 1-octanethiol and then modified by lipids (AuNP@lipid). In membrane surface-enhanced Raman spectroscopy (MSERS), both signals from 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) and Chol molecules were enhanced, depending on preparation conditions (size of AuNPs and lipid/AuNP ratio). The enhancement factors (EFs) were calculated to estimate the efficiency of AuNPs on Raman enhancement. The size of AuNP100nm@lipid was 152.0 ± 12.8 nm, which showed an surface enhancement Raman spectrum with an EF2850 value of 111 ± 9. The size of AuNP5nm@lipid prepared with a lipid/AuNP ratio of 1.38 × 104 (lipid molecule/particle) was 275.3 ± 20.2 nm, which showed the highest enhancement with an EF2850 value of 131 ± 21. On the basis of fluorescent probe analyses, the membrane fluidity and polarity of AuNP@lipid were almost similar to DOPC/Chol liposome, indicating an intact membraneof DOPC/Chol after modification with AuNPs. Finally, the membraneproperties of AuNP@lipid systems were also discussed on the basisof the obtained MSERS signals.
机译:金纳米粒子(AuNP)取决于其大小,具有局部表面等离振子共振峰,通常用于表面增强拉曼散射(SERS)。为了通过SERS获得掺入胆固醇(Chol)的脂质膜的信息,首先将AuNPs(5,100 nm)通过1-辛烷硫醇官能化,然后通过脂质(AuNP @ lipid)进行修饰。在膜表面增强拉曼光谱(MSERS)中,取决于制备条件(AuNP的大小和脂质/ AuNP的比值),来自1,2-二油酰基-sn-甘油-3-磷酸胆碱(DOPC)和Chol分子的信号均得到增强。 。计算增强因子(EFs)以估计AuNPs对拉曼增强的效率。 AuNP100nm @脂质的尺寸为152.0±12.8nm,其显示出表面增强拉曼光谱,EF2850值为111±9。脂质/ AuNP比为1.38×10 4制备的AuNP5nm @脂质的尺寸/ sup>(脂质分子/颗粒)为275.3±20.2 nm,以EF2850值为131±21表现出最高的增强。根据荧光探针分析,AuNP @脂质的膜流动性和极性几乎与DOPC / Chol脂质体,表明膜完整AuNPs修饰后的DOPC / Chol的制备。最后,膜在此基础上还讨论了AuNP @脂质系统的性质获得的MSERS信号。

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